ChemicalBook > CAS DataBase List > Trimethylsilyl cyanide

Trimethylsilyl cyanide

Product Name
Trimethylsilyl cyanide
CAS No.
7677-24-9
Chemical Name
Trimethylsilyl cyanide
Synonyms
TMSCN;TRIMETHYLSILANECARBONITRILE;trimethylsilylformonitrile;CYANOTRIMETHYLSILANE;TRIMETHYLCYANOSILANE;TRIMETHYLSILYLNITRILE;DK897;Trimethylsilanecar;Trimethyl cyanogen;CYANTRIMETHYLSILANE
CBNumber
CB1667134
Molecular Formula
C4H9NSi
Formula Weight
99.21
MOL File
7677-24-9.mol
More
Less

Trimethylsilyl cyanide Property

Melting point:
8-11 °C(lit.)
Boiling point:
114-117 °C(lit.)
Density 
0.793 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.392(lit.)
Flash point:
34 °F
storage temp. 
Inert atmosphere,2-8°C
solubility 
Miscible with organic solvents.
form 
liquid
Specific Gravity
0.744
color 
Yellow
Water Solubility 
reacts
Sensitive 
Moisture Sensitive
Hydrolytic Sensitivity
8: reacts rapidly with moisture, water, protic solvents
BRN 
1737612
Exposure limits
NIOSH: IDLH 25 mg/m3
Stability:
Moisture Sensitive
InChIKey
LEIMLDGFXIOXMT-UHFFFAOYSA-N
CAS DataBase Reference
7677-24-9(CAS DataBase Reference)
EPA Substance Registry System
Silanecarbonitrile, trimethyl- (7677-24-9)
More
Less

Safety

Hazard Codes 
F,T+,T,N
Risk Statements 
11-26/27/28-29-50/53
Safety Statements 
16-36/37/39-45-61-28A-26
RIDADR 
UN 3384 6.1/PG 1
WGK Germany 
3
10-21
Hazard Note 
Highly Flammable/Toxic
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29310095
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
73328
Product name
Trimethylsilyl cyanide
Purity
technical, ≥95% (GC)
Packaging
50mL
Price
$237
Updated
2024/03/01
Sigma-Aldrich
Product number
73328
Product name
Trimethylsilyl cyanide
Purity
technical, ≥95% (GC)
Packaging
250ML
Price
$908
Updated
2024/03/01
Sigma-Aldrich
Product number
212849
Product name
Trimethylsilyl cyanide
Purity
98%
Packaging
5g
Price
$56.1
Updated
2024/03/01
Sigma-Aldrich
Product number
212849
Product name
Trimethylsilyl cyanide
Purity
98%
Packaging
25g
Price
$136
Updated
2024/03/01
Alfa Aesar
Product number
A19598
Product name
Trimethylsilyl cyanide, 97%
Packaging
5g
Price
$56.8
Updated
2024/03/01
More
Less

Trimethylsilyl cyanide Chemical Properties,Usage,Production

Chemical Properties

Trimethylsilyl cyanide (TMSCN) is a commercial reagent used as cyanide source for nucleophilic reactions. It is a clear colorless to yellow liquid, moisture sensitive, with a boiling point of 114–117 °C, which was first synthetized by the reaction of trimethylsilicon halides TMSX and AgCN in 1952.

TMSCN is a versatile reagent that can be used in several different reactions, but it is generally used in nucleophilic additions to aldehydes, ketones and imines to form cyanohydrin silyl ethers (Scheme 1a) and α-aminonitriles in Strecker-type reactions (Scheme 1b).
Reactions of Trimethylsilyl Cyanide

Physical properties

Trimethylsilane cyanide is a colorless volatile liquid with almond odor, soluble in most organic solvents, such as dichloromethane, chloroform, etc.; it reacts violently with protic solvents such as water. This compound is used in organic synthesis as a replacement reagent for highly toxic HCN to introduce cyano groups into molecules.

Uses

Reacts with aldehydes and ketones to give cyanohydrin-TMS ethers which can be reduced to β-aminoethyl alcohols.
Trimethylsilyl cyanide (TMSCN) participates in carbonyl aminomethylation via α-silyloxy nitriles.
TMSCN can be used as a reagent in the:
Trimethylsilyl cyanide was used in the second step of an oxidative Michael addition of cyanide anion to Baylis–Hillman adducts. The importance of the addition of cyanide to α,β-unsaturated carbonyl derivatives is that the products can be converted into a variety of compounds including γ-aminobutyric acids. The reaction took place in a liquid ionic medium ([bmim]Br), which was reused several times without losing its activity. The β-cyano carbonyl compounds were obtained with high regioselectivity and yields (>79%).

Cyanosilylation of carbonyl compounds using various catalysts.
Synthesis of α-aminonitriles by one-pot, three-component Strecker reaction of ketones with various amines using Brønsted acid catalyst.
Cyanation of aryl halides using palladium-complex as a catalyst.

Uses

Cyanotrimethylsilane is a highly versatile reagent that reacts with a multitude of functional groups to yield an array of products and/or highly valuable synthetic intermediates.
Aldehydes and ketones are readily transformed into the corresponding cyanohydrin trimethylsilyl ethers when treated with cyanotrimethylsilane in the presence of Lewis acids (eq 1), triethylamine,or solid bases such as CaF2 or hydroxyapatite. The products can be readily hydrolyzed to the corresponding cyanohydrins. The cyanosilylation of aromatic aldehydes can be achieved with high enantioselectivity in the presence of catalytic amounts of a modified Sharpless catalyst consisting of titanium tetraisopropoxide and L-(+)-diisopropyl tartrate (eq 2).Catalysis with chiral titanium reagents yields aliphatic and aromatic cyanohydrins in high chemical and optical yields (eq 3). Cyanohydrins can be subsequently transformed into a variety of useful synthetic intermediates (eq 4).

Uses

Trimethylsilyl Cyanide is used as a reagent in the synthesis of optically active cyanohydrins. Used in the preparation of Reissert compounds, which represent reactive polyamides. Toxic to humans.

Preparation

Trimethylsilyl cyanide, (CH3)3 Si-CN, is obtained by reacting trimethylsilyl chloride with an approximately equimolar amount of an alkali metal cyanide in the absence of water and in the presence of catalytic, sub-stoichiometric amounts of both an alkali metal iodide and N-methylpyrrolidone, at a temperature of from 15°-25° C.
Trimethylsilyl cyanide is very toxic. All reactions in this sequence should be carried out in a hood.
Preparation of trimethylsilyl cyanide
TRIMETHYLSILYL CYANIDE: CYANOSILATION OF p-BENZOQUINONE

Reactions

Trimethylsilyl cyanide is a useful silicon reagent which reacts readily with aldehydes and ketones in the presence of catalytic amounts of Lewis acids or of cyanide ion, to give the trimethylsilyl ethers of the corresponding cyanohydrins (Evans,Carroll and Truesdale,1974).Even normally unreactive ketones react readily with trimethylsilyl cyanide due to the formation of the strong Si-O bond which displaces the equilibrium in favour of the derivative.The reaction provides a valuable alternative to the base-catalysed addition of hydrogen cyanide to carbonyl compounds which often gives only poor yields.Tetralone,for example,is reported not to form a cyanohydrin, but it gives a trimethylsilyl derivative in excellent yield.The silylated cyanohydrins can be hydrolysed to a-hydroxy acids(Corey, Crouse and Anderson,1975) and on reduction with lithium aluminium hydride they afford the corresponding 3-amino alcohols in excellent yield.This sequence provides a better route to these valuable intermediates (they are used in the ring expansion of cyclo- alkanones)than the classical methods through reaction of hydrogen cyanide or nitromethane with the carbonyl compound.The derivatives from aromatic aldehydes are excellent acyl anion equivalents and have been used in 'umpolung' conversion of aldehydes into ketones and acyloins by reaction of the derived anions with alkyl halides and aldehydes or ketones (Deuchert et al,1979;Hnig and Wehner,1979).

Purification Methods

The material should have only one sharp signal in the 1H NMR (in CCl4 with CHCl3 as internal standard) : 0.4ppm and IR with max at 2210cm1 [McBride & Beachall J Am Chem Soc 74 5247 1952, Prober J Am Chem Soc 77 3224 1955]; otherwise purify it by fractionating through an 18 x 1/4inch column. [Evers et al. J Am Chem Soc 81 4493 1959.] It has also been carefully distilled using a 60cm vacuum jacketed column. If the volume of sample is small, the cyanide can be chased (in the distillation) with xylene that had been previously distilled over P2O5. It is HIGHLY TOXIC and FLAMMABLE. [Evans et al. J Org Chem 39 914 1974, Beilstein 4 IV 3893.]

More
Less

Trimethylsilyl cyanide Suppliers

Hubei Huangbo Medical Technology Co., LTD
Tel
15231819181
Email
huangboniudong@163.com
Country
China
ProdList
6
Advantage
58
HANGZHOU HUINUO PHARMA & TECHNOLOGY CO., LTD
Tel
0571-0571-0571-88003882 13777838306
Email
hfangjin7205@126.com
Country
China
ProdList
37
Advantage
58
Nanjing Yili Biotechnology Co., Ltd.
Tel
15251862682
Email
2880300874@qq.com
Country
China
ProdList
8134
Advantage
58
Zhejiang zetian fine chemical co. LTD
Tel
0571-87322520 18957127338
Email
June@zetchem.com
Country
China
ProdList
398
Advantage
58
Henan Wanxiang Chemical Industry Co., Ltd.
Tel
0371-56669001 13949088811
Fax
0371-56669008
Email
Sales@58chem.cn
Country
China
ProdList
89
Advantage
62
Jinan LuoHe PharmaTech Co., Ltd.
Tel
0531-68658065 15726150375
Fax
0531-68658065
Email
jinanluohe@163.com
Country
China
ProdList
494
Advantage
58
Nantong Enwang New Materials Co.,Ltd
Tel
18912257866杨 18912257866
Email
739904460@qq.com
Country
China
ProdList
49
Advantage
58
XPERTICK (SHANDONG) BIO-PHARMACEUTICAL CO., LTD
Tel
21-58999881 15623240527
Email
emily@xtick.cn
Country
China
ProdList
72
Advantage
58
Qingdao Baiyi Chemical Co., Ltd
Tel
13953303907
Email
2338367690@qq.com
Country
China
ProdList
112
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
More
Less

View Lastest Price from Trimethylsilyl cyanide manufacturers

Shanghai UCHEM Inc.
Product
Trimethylsilyl cyanide 7677-24-9
Price
US $14.00-170.00/g
Min. Order
25g
Purity
0.98
Supply Ability
100kg
Release date
2023-11-15
Hebei Weibang Biotechnology Co., Ltd
Product
Trimethylsilyl cyanide 7677-24-9
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-31
Hebei Yanxi Chemical Co., Ltd.
Product
Trimethylsilyl cyanide 7677-24-9
Price
US $50.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10000
Release date
2023-10-30

7677-24-9, Trimethylsilyl cyanideRelated Search:


  • TRIMETHYLSILYL CYANIDE FOR SYNTHESIS
  • trimethylsilylformonitrile
  • trimethylsilylmethanenitrile
  • trimethyl-silanecarbonitril
  • trimethylsilycyanide
  • TMSCN
  • TRIMETHYLSILANECARBONITRILE
  • TRIMETHYLSILYL CYANIDE
  • TRIMETHYLSILYLNITRILE
  • TRIMETHYLCYANOSILANE
  • TriMethylsilyl Cyanide, 97%, SpcSeal
  • Three Methyl cyanide silane
  • Trimethylsilanecar
  • CYANOTRIMETHYLSILANE
  • CYANTRIMETHYLSILANE
  • Cyanotrimethylsilane~TMSCN
  • Trimethyl Silane Cyanide
  • trimethylsilylcarbonitrile
  • Trimethylsilycyanidel
  • Trimethylsilylcyanide,97%
  • Trimethylsilylcyanide(Trimethylsilylnitrile)
  • Silanecarbonitrile, trimethyl-
  • Trimethylsilyl cyanide (Cyanotrimethylsilane)
  • Trimethylsilylcyanid
  • Trimethycyanosilane
  • TRIMETHYLSILYLCYANIDE (99%)
  • Trimethylsilyl cyani
  • Trimethylsilyl cyanide,98%
  • Trimethylsilyl cyanide ,93%
  • Trimethylsilyl cyanide, 96%, for synthesis
  • Trimethyl cyanogen
  • Trimethylsilylcarbonitril
  • N-(Trimethylsilyl)imidazole (TSIM)
  • Trimethylsilyl cyanide, 98%, AcroSeal&trade
  • DK897
  • 7677-24-9
  • CH33SiCN
  • C4H9NSi
  • C1 to C5
  • Building Blocks
  • Silicon Compounds (for Synthesis)
  • Si-(C)4 Compounds
  • Si (Classes of Silicon Compounds)
  • Organic Building Blocks
  • Nitrogen Compounds
  • Cyanides/Nitriles
  • Si (Classes of Silicon Compounds)
  • Si-(C)4 Compounds
  • Silicon Compounds (for Synthesis)
  • Synthetic Organic Chemistry
  • Small molecule
  • Building Blocks
  • C1 to C5
  • Chemical Synthesis
  • Cyanides/Nitriles
  • Nitrogen Compounds
  • Organic Building Blocks
  • 7677-24-9